Prader–Willi syndrome

External resources

Library of Congress ID	sh85106050[1] referuar si: Prader-Willi syndrome
SNOMED CT ID	89392001
Store medisinske leksikon ID	Prader-Willis_syndrom
MeSH descriptor ID	D011218[2] referuar si: Prader-Willi Syndrome
Encyclopædia Britannica Online ID	science/Prader-Willi-syndrome referuar si: Prader-Willi syndrome emri i autorit si varg: Sarah E. Boslaugh
Quora topic ID	Prader-Willi-Syndrome[3]
YSO ID	18144[4] referuar si: Prader-Willin oireyhtymä, Prader-Willis syndrom, Prader-Willi syndrome
PatientsLikeMe condition ID	prader-willi-syndrome
Miraheze article ID	Prader-Willi_Syndrome
DiseasesDB	10481
GeneReviews ID	NBK1330
Orphanet ID	739
Patientplus ID	prader-willi-syndrome-pro[5]
Disease Ontology ID	DOID:11983[2]
NDL Authority ID	01179976
eMedicine ID	947954
WikiProjectMed ID	Prader–Willi syndrome
Genetics Home Reference Conditions ID	prader-willi-syndrome
MedlinePlus ID	001605
Freebase ID	/m/0fb3f[6]
OMIM ID	176270[2]
MeSH tree code	C10.597.606.360.690 C16.131.077.730 C16.131.260.700 C16.320.180.700 C18.654.726.750.500.740 C16.320.447.500
ICD-10-CM	Q87.1[2]
Wolfram Language entity code	Entity["Disease", {"ICDNine759.81", "Primary"}]
JSTOR topic ID	prader-willi-syndrome
WikiKids ID	Syndroom_van_Prader-Willi
NHS Health A to Z ID	prader-willi-syndrome
UMLS CUI	C0032897[2] C0265222[7]
GARD rare disease ID	5575[2]
WikiSkripta article ID	8491
BNCF Thesaurus ID	67274 referuar si: Sindrome di Prader-Willi alternative name: PWS, Sindrome di Prader Willi
ICD-11 (foundation)	393773440
GND ID	4201277-6
ICD-11 ID (MMS)	LD90.3 referuar si: Prader-Willi syndrome
KEGG ID	H00478
identifikues i BNF	12468434q[8] referuar si: Prader-Labhart-Willi, Syndrome de
National Library of Israel J9U ID	987007531653205171[9]

instancë e

designated intractable/rare disease^[10]

rare disease

class of disease

nënklasë e

chromosomal disease^[2]

sindromë^[2]

syndromic obesity

sëmundje

video

gjuha e veprës ose emrit: anglisht

emëruar prej

Andrea Prader^[11]

Heinrich Willi^[11]

health specialty

medical genetics

Pediatria

neurologjia

drug or therapy used for treatment

somatrem^[12]

genetic association

SNRPN^[13]

NDN^[14]

të dhëna të jashtme në dispozicion në

http://www.nanbyou.or.jp/entry/4768^[10]

gjuha e veprës ose emrit: japonisht

montage image

on focus list of Wikimedia project

WikiProject Medicine

skemë

ICD-9-CM

759.81^[2]

NCI Thesaurus ID

C75463^[2]

përputhje e saktë

http://purl.obolibrary.org/obo/DOID_11983^[2]

http://identifiers.org/doid/DOID:11983^[15]

kategoria në Commons

Prader-Willi syndrome

Reference

1. ^ GND
2. ^ ^{a b c d e f g h i j k} Disease Ontology, 15 maj 2019, DOID:11983
3. ^ Quora
4. ^ YSO-Wikidata mapping project, 8 shkurt 2022
5. ^ http://www.patient.co.uk/patientplus/p.htm
6. ^ Freebase Data Dumps, 28 tetor 2013
7. ^ UMLS 2023, 25 maj 2023, inferred by common MeSH mappings on source and on Wikidata
8. ^ Nuovo soggettario, https://thes.bncf.firenze.sbn.it/termine.php?id=67274, 18 qershor 2021
9. ^ Biblioteka Kombëtare e Izraelit
10. ^ ^{a b} https://ddrare.nibiohn.go.jp/, 17 maj 2019
11. ^ ^{a b} https://www.ncbi.nlm.nih.gov/books/NBK1330/
12. ^ N0000147652, 13 dhjetor 2016, NDF-RT, anglisht
13. ^ Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients
14. ^ Association of acetylated histones with paternally expressed genes in the Prader--Willi deletion region
15. ^ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233